The Compliance Companion
Who Is the Company Behind The Compliance Companion?
- Seller: The Compliance Companion
- Year Founded: 2011
- HQ Location: Cardiff, GB
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LinkedIn® Page: www.linkedin.com
1 employees on LinkedIn®
Total Products under this Category: 389
Last updated: September 01, 2026
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Highlighted products: MasterControl Quality Management System, Qualio, Redzone, EASE, Octave Reliance (ETQ Reliance), SAP Cloud ERP (SAP S/4HANA Cloud), QT9 QMS, and Ideagen Quality Management.
Underlying data: [Grid® JSON](https://www.g2.com/categories/quality-management-qms/grids.json?focus%5B%5D=mastercontrol-quality-management-system&focus%5B%5D=qualio&focus%5B%5D=qad-redzone&focus%5B%5D=ease-inc-ease&focus%5B%5D=octave-reliance-etq-reliance&focus%5B%5D=sap-cloud-erp-sap-s-4hana-cloud&focus%5B%5D=qt9-qms&focus%5B%5D=ideagen-quality-management)
The TilliT Digital Manufacturing Operations software enables fully paperless operations by integrating production, quality, and maintenance processes in a single low-code cloud platform. Light-weight and easily deployed TilliT combines asset performance monitoring, OEE, work order execution, quality management, knowledge management and production scheduling driven by workflow automation and AI optimization. By connecting to existing equipment or by using our suite of IoT sensors, TilliT brings together people, products, processes and equipment for complete operational control.
Average Rating: 4.0/5.0
Total Reviews: 1
Rating: 4.0/5.0 stars
— Andres Camilo S.
Enterprise field workforce management and safety platform integrating electronic Permit to Work ePTW, LOTO, and CMMS tracking.
TQA Cloud is a quality management software that is the simple easy to use QMS that can be adapted to fit any business, any standard ISO 9001, ISO 14001, ISO 45001, API and ASME
ManualMaster Trevally is next-generation QHSE and quality-management software that unifies the entire Plan-Do-Check-Act loop in one configurable platform, available as SaaS or on-premises. By centralising policies, processes and improvement data, Trevally helps organisations move as cohesively—and decisively—as the schooling fish that inspired its name. At its core, Trevally delivers rock-solid document control with automated versioning, full audit trails and electronic signatures, ensuring every colleague receives “the right information at the right time and in the right place.” Around that foundation sits a rich suite of modules that can be activated as you grow: risk and standard management, process mapping, QA registrations, CAPA, incident and complaint handling, audit and deviation tracking, tasks & actions, plus role-based dashboards with real-time KPIs and reports. Smart web forms and Q-Learning features make it easy to capture data and raise competence across the business. Trevally is engineered for the compliance realities of regulated industries. ISO-27001-certified hosting, SSO, MFA and granular permissions keep data secure, while multilingual interfaces, mobile access and an open API promote broad user adoption and seamless ecosystem integration. Powerful reporting turns scattered QHSE evidence into actionable insight, accelerating both internal and external audits and supporting standards such as ISO 9001, ISO 13485 and GMP. Unlike generic content repositories, Trevally arrives with more than thirty years of ManualMaster expertise baked in. New customers receive personalised onboarding, live and online training, and responsive Dutch- and English-speaking support that continues long after go-live—so teams spend time improving processes, not wrestling with software. Proven in construction, chemicals, laboratories, food, healthcare, logistics and the public sector, Trevally scales from single sites to global enterprises and adapts as requirements evolve. Whether you need a modern web portal for frontline workers or an on-premise deployment behind your own firewall, Trevally equips quality professionals with the control, visibility and agility to drive continual improvement—without ever compromising compliance.
Tricorn: QMS is a quality management software that deals with all aspects of running a total quality management system to ISO9001:2015/AS9100 and other equivalent quality standards.
Support accreditation and ongoing compliance with ISO 9001 (Quality), ISO 45001 (Safety), and ISO 14001 (Environment). Manage policies, procedures, internal audits, non-conformance reports, and continual improvement actions within a centralised, structured framework.
SG Systems Global’s V5 MES Manufacturing Execution System is a flexible manufacturing execution platform that replaces manual processes with digital, real-time control. Built for manufacturers across industries, V5 connects every stage of production — from material receiving to final shipment — with instant visibility, barcode-led accuracy, and automated compliance. Key Features: Complete lot and batch traceability – Search forward or backward in seconds for rapid recalls, regulatory audits, or customer inquiries. Barcode-based error prevention – Verify correct materials, quantities, and processes to eliminate costly production mistakes. Digitized production workflows – Provide operators with guided, step-by-step instructions, timers, and approvals for consistent results. Real-time quality checks – Record inspections as work happens, escalate deviations, and track corrective actions. Advanced warehouse management – Control inventory locations with zoning for allergens, temperature, quarantine, and FIFO/LIFO rules. GMP & 21 CFR Part 11 readiness – Maintain secure, audit-ready electronic records with controlled access, e-signatures, and data integrity safeguards. With ERP integration, configurable workflows, and scalable deployment, V5 MES helps manufacturers improve efficiency, reduce waste, and stay compliant without slowing production.
Verifarma QMS is Verifarma’s Quality Management System, specifically designed for the pharmaceutical, veterinary, and life sciences industries. The solution centralizes, digitizes, and controls all key quality processes, ensuring compliance with local and international regulations while promoting continuous improvement. The platform enables integrated management of deviations, CAPAs, change controls, audits, documentation, training, and risk management, providing full traceability, version control, and audit-ready records. Verifarma QMS replaces manual and fragmented processes with a unified, validated environment aligned with regulatory best practices. Designed to scale alongside organizational growth, Verifarma QMS adapts to companies of different sizes and regulatory frameworks, helping quality teams reduce errors, improve operational efficiency, and ensure patient safety.
Vintara QMS provides a fully automated, web-based enterprise quality management solution. Vintara QMS is a centralized database of dashboards, performance KPIs, content, documents, and processes designed to manage and document the quality process and compliance with international standards.